MEDICAL DEVICES
All establishments that are involved in the production and distribution of medical devices intended for use in Mexico are required to register their products before the COFEPRIS.
We offer the best classification strategy for your products in order to save resources and time during product quality-related assessments
We submit and monitor the status of your applications before COFEPRIS to ensure a positive response from the Authority in a timely manner
We have an expert team that will gather the precise information required for an agile and succesful evaluation of your applications.
Focus on your business: We are your representative before COFEPRIS as registration holders and take over all procedures and operational activities to ensure continuity of your registration/s. In this way, you can also expand your supplier scheme in Mexico.